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Minimal renal toxicity after Rituximab DHAP with a modified cisplatin application scheme in patients with relapsed or refractory diffuse large B-cell lymphoma

Lisenko, Katherina ; McClanahan, F. ; Schöning, Tilman ; Schwarzbich, Mark Alexander ; Cremer, Martin ; Dittrich, Tobias ; Ho, Anthony D. ; Witzens-Harig, Mathias

In: BMC Cancer, 16 (2016), Nr. 267. pp. 1-7. ISSN 1471-2407

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Download (1MB) | Lizenz: Creative Commons LizenzvertragMinimal renal toxicity after Rituximab DHAP with a modified cisplatin application scheme in patients with relapsed or refractory diffuse large B-cell lymphoma by Lisenko, Katherina ; McClanahan, F. ; Schöning, Tilman ; Schwarzbich, Mark Alexander ; Cremer, Martin ; Dittrich, Tobias ; Ho, Anthony D. ; Witzens-Harig, Mathias underlies the terms of Creative Commons Attribution 3.0 Germany

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Abstract

Background: Rituximab (R) in combination with DHAP is a widely accepted salvage regimen for patients with relapsed or refractory diffuse large B-cell lymphoma (DLBCL). A common adverse effect of this protocol is renal toxicity which may result in treatment discontinuation. Assuming that a lower single dose of cisplatin over several days would reduce renal toxicity, our institution has chosen to administer cisplatin in a dosage of 25 mg/m2 per day as a 3-h infusion over 4 consecutive days. Methods: In this study, we analyzed the renal function of 122 patients with relapsed or refractory DLBCL treated with R-DHAP at our institution. Overall, 256 R-DHAP cycles were administered. 31 (25 %), 61 (50 %), 14 (12 %) and 16 (13 %) patients received one, two, three or four R-DHAP courses, respectively. Results: A glomerular filtration rate (GFR) decrease was observed after each R-DHAP cycle. However, in none of the subgroups the median GFR was lower than 60 ml/min/1.73 m2. In most patients, only renal impairment stage I and II was observed. Renal impairment stage III was seen in 10 % and stage IV only in 1 % of patients. Conclusion: We conclude that a modified R-DHAP regimen with administration of cisplatin 25 mg/m2 over 4 consecutive cycles leads only to minimal renal toxicity.

Document type: Article
Journal or Publication Title: BMC Cancer
Volume: 16
Number: 267
Publisher: BioMed Central; Springer
Place of Publication: London; Berlin; Heidelberg
Date Deposited: 15 Apr 2016 13:17
Date: 2016
ISSN: 1471-2407
Page Range: pp. 1-7
Faculties / Institutes: Medizinische Fakultät Heidelberg > Medizinische Universitäts-Klinik und Poliklinik
DDC-classification: 610 Medical sciences Medicine
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